Canonical Allele Identifier: CA595293837

Gene: PLCE1

Linked Data

• dbSNP Id: rs1371974126
• gnomAD v2: 10-96053411-T-A
• MyVariant Identifiers: chr10:g.96053411T>A (hg19) ; chr10:g.94293654T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293654T>A , CM000672.2:g.94293654T>A	GRCh38
NC_000010.10:g.96053411T>A , CM000672.1:g.96053411T>A	GRCh37
NC_000010.9:g.96043401T>A	NCBI36
NG_015799.1:g.304666T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4243+15T>A	ENSP00000360426.1:n.4243+15T>A
ENST00000685253.1:c.*1710+15T>A	ENSP00000509405.1:n.*1710+15T>A
ENST00000685889.1:n.1902+15T>A
ENST00000686807.1:n.586+15T>A
ENST00000686954.1:c.*451+15T>A	ENSP00000508416.1:n.*451+15T>A
ENST00000688810.1:c.4195+15T>A	ENSP00000509140.1:n.4195+15T>A
ENST00000689233.1:n.9375+15T>A
ENST00000690340.1:n.2840+15T>A
ENST00000692286.1:c.5036-4725T>A	ENSP00000509490.1:n.5036-4725T>A
ENST00000692396.1:c.5119+15T>A	ENSP00000508605.1:n.5119+15T>A
ENST00000371380.8:c.5167+15T>A MANE Select	ENSP00000360431.2:n.5167+15T>A
ENST00000371385.8:c.4141+15T>A	ENSP00000360438.4:n.4141+15T>A
ENST00000674738.1:c.3722+15T>A
ENST00000674827.1:c.3283+15T>A	ENSP00000502523.1:n.3283+15T>A
ENST00000675218.1:c.4243+15T>A	ENSP00000501910.1:n.4243+15T>A
ENST00000675487.1:c.*1100+15T>A	ENSP00000502340.1:n.*1100+15T>A
ENST00000675718.1:c.4436+15T>A
ENST00000676102.1:c.4012+15T>A	ENSP00000502811.1:n.4012+15T>A
ENST00000260766.7:c.5167+15T>A	ENSP00000260766.3:n.5167+15T>A
ENST00000371375.1:c.4243+15T>A	ENSP00000360426.1:n.4243+15T>A
ENST00000371380.7:c.5167+15T>A	ENSP00000360431.2:n.5167+15T>A
ENST00000371385.7:c.4243+15T>A	ENSP00000360438.3:n.4243+15T>A
NM_001165979.2:c.4243+15T>A	NP_001159451.1:n.4243+15T>A
NM_001288989.1:c.5119+15T>A	NP_001275918.1:n.5119+15T>A
NM_016341.3:c.5167+15T>A	NP_057425.3:n.5167+15T>A
XM_006717885.2:c.5209+15T>A	XP_006717948.1:n.5209+15T>A
XM_006717886.2:c.5209+15T>A	XP_006717949.1:n.5209+15T>A
XM_006717888.2:c.5206+15T>A	XP_006717951.1:n.5206+15T>A
XM_006717889.2:c.5161+15T>A	XP_006717952.1:n.5161+15T>A
XM_006717890.1:c.4285+15T>A	XP_006717953.1:n.4285+15T>A
XM_011539849.1:c.5209+15T>A	XP_011538151.1:n.5209+15T>A
XM_011539850.1:c.4054+15T>A	XP_011538152.1:n.4054+15T>A
XM_006717885.4:c.5209+15T>A	XP_006717948.1:n.5209+15T>A
XM_006717888.4:c.5206+15T>A	XP_006717951.1:n.5206+15T>A
XM_006717889.4:c.5161+15T>A	XP_006717952.1:n.5161+15T>A
XM_006717890.3:c.4285+15T>A	XP_006717953.1:n.4285+15T>A
XM_011539849.3:c.5209+15T>A	XP_011538151.1:n.5209+15T>A
XM_011539850.3:c.4054+15T>A	XP_011538152.1:n.4054+15T>A
XM_017016310.2:c.5209+15T>A	XP_016871799.1:n.5209+15T>A
XM_017016311.2:c.5209+15T>A	XP_016871800.1:n.5209+15T>A
XM_017016312.2:c.4195+15T>A	XP_016871801.1:n.4195+15T>A
NM_001288989.2:c.5119+15T>A	NP_001275918.1:n.5119+15T>A
NM_016341.4:c.5167+15T>A MANE Select	NP_057425.3:n.5167+15T>A